Adhesive tape for rechargeable battery and rechargeable battery including same
US-2024372219-A1 · Nov 7, 2024 · US
US9725543B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9725543-B2 |
| Application number | US-201414540551-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 13, 2014 |
| Priority date | Mar 6, 2009 |
| Publication date | Aug 8, 2017 |
| Grant date | Aug 8, 2017 |
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The present invention relates to hexafluoropropylene oxide polymer composition and a process of preparing ofhexafluoropropylene oxide polymer by an anionic polymerization, and in particular the hexafluoropropylene oxide polymer composition comprises an anionic initiator, a polar solvent, hexafluoropropylene and hexafluoropropylene oxide. The hexafluoropropylene oxide polymer is prepared under particular reaction conditions by using the composition, hexafluoropropylene oxide poylymer prepared by using the composition according to a preparation process herein has a weight average molecular weight (Mw) of 1,500-4,000 at −10 to 20° C.
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What is claimed is: 1. A process of preparing hexafluoropropylene oxide polymer, the process comprising: (a) preparing hexafluoropropylene dimer and hexafluoropropylene trimer by introducing hexafluoropropylene to a mixture of an anionic initiator and a polar solvent at 20-40° C. and under nitrogen altiiosphere, wherein the hexafluoropropylene dimer and hexafluoropropylene trimer are present in a weight ratio of 20-40:80-60based on the total weight of the hexafluoropropylene dimer and hexafluoropropylene trimer; and (b) preparing hexafluoropropylene oxide polymer of Formula 1 by introducing hexafluoropropylene oxide at an average rate of 1.5-2.5 g/min at −10 to 20° C. to a reactor after the step (a) is conducted, wherein the amount of hexafluoropropylene oxide is 300-700 weight parts relative to 100 weight parts of the hexafluoropropylene dimer and hexafluoropropylene trimer: CF 3 CF 2 CF 2 O(CF(CF 3 )CF 2 O) n CF(CF 3 )COF:wherein n is an integer of 8-25. [Formula 1] 2. The process of preparing hexafluoropropylene oxide polymer of claim 1 , wherein the hexafluoropropylene dimer is at least one selected from the group consisting of 1,1,1,2,3,4,5,5,5-nonafluoro-4-(trifluoromethyl)pent-2-ene and 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-2-ene, and the hexafluoropropylene trimer is 1,1,1,3,4,5,5,5-octafluoro-2,4-bis(trifluoromethyl)pent-2-ene. 3. The process of preparing hexafluoropropylene oxide polymer of claim 1 , wherein a weight average molecular weight (Mw) of the hexafluotopropylene oxide polymer as measured at −10 to 20° C. is 1,500-4,000. 4. The process of preparing hexafluoropropylene oxide polymer of claim 2 , wherein a weight average molecular weight (Mw) of the hexafluoropropylene oxide polymer as measured at −10 to 20° C. is 1,500-4,000.
Hexyfluoropropene · CPC title
containing fluorine · CPC title
Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring · CPC title
containing halogens · CPC title
Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule · CPC title
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